Validation Specialist Jobs

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52 Validation Specialist jobs found on Monster.

Jobs 1 to 20 of 52
Join STERIS in its vision to see the world free from Infection and Contamination as a Equipment Validation Specialist Biotest Laboratories has an exciting opportunity for an experienced Equipment Validation Specialist! We're seeking an experienced, enthusiastic, energetic self-starter to join our team in our expanding business. If you have experience with equipment qualifications for GCs, autocl...
MIRUS CONSULTING GROUP Engineers /Validation Specialists 10 available positions Seeks experienced Engineers - Fully Bilingual (English and Spanish) - Excellent technical writing skills (is a MUST) - Must BS Degree in Engineering (EIT) - At least two (2) years experience in Commissioning, Validation, and Qualification; OR three (3) years experience in the Biotech, Pharmaceutical, Medical De...
• Develop, implement and maintain process validation procedures to current regulatory, industry, and corporate standards. Lead Validation Projects. Coordinate validation activities with Operations, Logistics, Engineering, and Project Management groups to ensure their efficient completion. • Design, execute, document, and generally oversee programs intended to ensure the continued proper operation...
PharCom Solutions Corp. is looking for a Validation/ Qualification specialist with at least 5 years of experience in the pharmaceutical industry. Requisites: BS degree in engineering or sciences. Required experience: Strong knowledge on GMP regulations. Development and Execution of IQ/OQ/PQ for equipments, utilities and facilities. Process Validation Computer Validation Issue and revise St...
Company Confidential Amityville, NY, 11701
VALIDATION SPECIALIST –CLEANING QUALIFICATION Our Company We are a rapidly growing pharmaceutical manufacturer, with core competencies in the sterile injectable and ophthalmic sectors, and with many new products in development and awaiting FDA approval. In anticipation of long-term, substantial growth, we offer challenging, attractive career opportunities along with competitive salaries and comp...
The Associate Validation Specialist is primarily responsible for gathering and interpreting information and applying current industry standards for Equipment Qualification and/or Process Validation and/or Cleaning Validation practices for the Winchester facility in drafting protocols and reports. Specific Tasks, Duties and Responsibilities: • Drafting Protocols and reports for Equipment Validati...
Validation Specialist to lead automation qualification activities throughout the site on multiple automation platforms including PLC’s, DeltaV Distributed Control Systems, Andover Building Automation Systems, and other automation platforms as implemented on site. Qualification of automation includes all areas of the manufacturing operations, site GMP utilities, and support of capital projects. Thi...
Marten Transport Au Sable Forks, NY
Company Description: ProGXP is a professional services firm. Our firm offers professional on-site consulting services to the Pharmaceutical, Medical Device and Biotech industries. We offer a variety of on-site consulting services including Engineering, Technical Services, Validation, Quality Assurance, Compliance, Regulatory and Recruitment / Staffing services. We are poised to work with clients o...
Thermo Fisher Scientific Inc. Canoga Park, CA
Job Level Experienced Description: Posting date: September 15, 2014 Transplant Diagnostics (TDX) develops and distributes several lines of histocompatibility (HLA) typing tests utilizing both serological and molecular technologies. TDX also manufactures a comprehensive line of antibody detection products, laboratory instrumentation, and computer software that are used to simplify and automate te...
Global Employment Solutions, Inc. Toms River, NJ
Apply Now ? Apply to this Job Send me a message:I'm interested in your Job #1714353: Validation Specialist, Pharmaceutical Automation System job in Toms River, NJ. Please contact me about the position. Name: Email: Phone: Attach your resume Get Job alerts for jobs like this Become a Bullhorn Reach member and receive employment updates By providing us with your information, you agree to b...
Amerigroup York, PA
Overview: General Summary: This position will be responsible for performing validation of equipment and processes for the manufacturing and packaging operations. This includes, but is not limited to, identifying equipment and / or processes, preparing IQ (Installation Qualification) / OQ (Operational Qualification) / PQ (Production Qualification) protocols, performing testing, collecting samples...
Agilent Technologies Inc. Santa Rosa, CA, DK
Date Posted: 16/Sep/14 Requisition: 2054829 Job Title: QA Validation Specialist Description: We are expanding our QA department in Dako with two QA specialists to support the qualification and validation activities in the production and QC of IVD kit and reagents. Do you want to be a part of an international company that fight cancer and do you enjoy working with QA Validation? This could be yo...
Baxter International Inc Los Angeles, CA
Description Applies a solid understanding of theories/practices utilized by other disciplines outside the primary area of expertise toward the development of new or enhanced products or processes. Plans, executes, and functionally directs important engineering assignments, which require independent judgment. The position also requires expertise in validation theory and principles such as process ...
Church & Dwight Co Inc York, PA
Overview: General Summary: This position will be responsible for performing validation of equipment and processes for the manufacturing and packaging operations. This includes, but is not limited to, identifying equipment and / or processes, preparing IQ (Installation Qualification) / OQ (Operational Qualification) / PQ (Production Qualification) protocols, performing testing, collecting samples...
GE Transportation Other, AL
Role Summary/Purpose The Field Validation Specialist will be responsible for installation support, testing, and commissioning of GE field products and systems, with a concentration in GE ITCS systems. Essential Responsibilities In addition you will: Write and submit test and inspection plans and procedures Write and submit test and inspection reports Exercise document control over plans, rep...
Description CSC has an immediate position for a Computer Validation Specialist within the DOC Systems group. This position is located in Frederick, Maryland. Essential Job Functions Ensure IT infrastructure, hardware and software systems purchased by DVC for the regulated network are installed, perform and operate according to specifications and user requirements. Lead qualification and valida...
Thermo Fisher Scientific Inc. Canoga Park, CA, 91303
Posting date: September 15, 2014 Transplant Diagnostics (TDX) develops and distributes several lines of histocompatibility (HLA) typing tests utilizing both serological and molecular technologies. TDX also manufactures a comprehensive line of antibody detection products, laboratory instrumentation, and computer software that are used to simplify and automate testing procedures and final test eval...
Grifols, Inc. Emeryville, CA
Overview: Responsible for developing and validating release, in-process and cleaning methods in support of Novartis Diagnostic’s immunodiagnostic products. This role will interact with Technology Development, Manufacturing, Research & Development, Quality Control and Quality Assurance staff to ensure that method validation and transfer studies are appropriate for the methods’ intended use(s) and ...
Thermo Fisher Scientific Inc. Rockville, MD, 20850
Posting date: August 21, 2014 Position Summary : This position will be required to manage various software validation efforts throughout the company. This person will be viewed as the internal expert with regard to the FDA regulation 21 CFR Part 11. Key Responsibilities: % 1. Interpret and apply government regulations, guidance documents, and industry standards pertaining to the validation an...
The Associate Validation Specialist is primarily responsible for gathering and interpreting information and applying current industry standards for Equipment Qualification and/or Process Validation and/or Cleaning Validation practices for the Winchester facility in drafting protocols and reports. Specific Tasks, Duties and Responsibilities: • Drafting Protocols and reports for Equipment Validati...

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Regulations Compliance Associate

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$31,200.00 - $94,080.00
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(53 Respondents)
Source: Monster.com Careerbenchmarking Tool

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Bachelor's
46.9%
Master's
18.4%
Some College Coursework Completed
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6.1%
Doctorate
6.1%
Professional
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High School
4.1%
(49 Respondents)
Source: Monster.com Careerbenchmarking Tool

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